Benzo[b]thiophen-2-yl(5-bromo-2-fluorophenyl)methanol
97%
- Product Code: 123144
CAS:
1034305-11-7
| Molecular Weight: | 337.21 g./mol | Molecular Formula: | C₁₅H₁₀BrFOS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28347651 | |
| Melting Point: | Boiling Point: | 458.7±40.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed away from light |
Product Description:
This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active molecules, particularly those targeting therapeutic applications. Its structure, featuring both a benzo[b]thiophene and a substituted phenyl ring, makes it valuable for designing compounds with potential anti-inflammatory, antimicrobial, or anticancer properties. Researchers often employ it in the synthesis of complex molecules to study structure-activity relationships and optimize drug efficacy. Additionally, its functional groups allow for further chemical modifications, enabling the creation of diverse derivatives for screening in drug discovery programs.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $58.75 |
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| 0.250 | 10-20 days | $99.75 |
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| 1.000 | 10-20 days | $269.24 |
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| 5.000 | 10-20 days | $1,222.38 |
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Benzo[b]thiophen-2-yl(5-bromo-2-fluorophenyl)methanol
This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active molecules, particularly those targeting therapeutic applications. Its structure, featuring both a benzo[b]thiophene and a substituted phenyl ring, makes it valuable for designing compounds with potential anti-inflammatory, antimicrobial, or anticancer properties. Researchers often employ it in the synthesis of complex molecules to study structure-activity relationships and optimize drug efficacy. Additionally, its functional groups allow for further chemical modifications, enabling the creation of diverse derivatives for screening in drug discovery programs.
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